Electronic structure, cationic, and excited states of nitrogen-containing spiroborates.

Context: This paper presents the results of the study of the electronic structure and cationic and excited states of three spiroborate complexes (2-acetylacetonato-1,3,2-benzodioxaborol, its NH- and NMe-derivatives) and three corresponding ligands (acetylacetone, 4-aminopent-3-en-2-one, and 4-methylaminopent-3-en-2-one). Materials based on spiroborates are used in medicine, for example, as a drug carrier. In industry, spiroborate anions are used in ionic liquids and as alternative high performance lubricants.

Electronic Structure of NdFeCoB Oxide Magnetic Particles Studied by DFT Calculations and XPS.

Neodymium-iron-boron magnetic oxide powders synthesized by sol-gel Pechini method were studied by using X-ray photoelectron spectroscopy (XPS) and quantum chemical modeling. The powder structure was examined by using X-ray diffraction (XRD) and modeled by using density functional theory (DFT) approximation. The electronic structures of the core and valent regions were determined experimentally by using X-ray photoelectron spectroscopy and modeled by using quantum chemical methods.

Spectroscopic and quantum chemical study of difluoroboron β-diketonate luminophores: Isomeric acetylnaphtholate chelates.

The electronic structure and optical properties of the isomeric difluoroboron β-diketonates, 2,2-difluoro-4-methylnaphtho-[2,1-e]-1,3,2-dioxaborin (I) and 2,2-difluoro-4-methylnaphtho-[1,2-e]-1,3,2-dioxaborin (II), were studied by means of X-ray photoelectron, absorption and luminescence spectroscopies. The experimental results were interpreted using high-level ab initio quantum chemical computations, including the algebraic-diagrammatic construction method for the polarization propagator of the second and third orders (ADC(2) and ADC(3)), the outer-valence Green's function (OVGF) method, and the time-dependent density functional (TDDFT) approach. The X-ray photoelectron measurements were assigned in the entire energy range using the results of the Kohn-Sham orbital calculations which employed the B3LYP functional.

Boron difluoride dibenzoylmethane derivatives: Electronic structure and luminescence.

Electronic structure and optical properties of boron difluoride dibenzoylmethanate and four of its derivatives have been studied by X-ray photoelectron spectroscopy, absorption and luminescence spectroscopy and quantum chemistry (DFT, TDDFT). The relative quantum luminescence yields have been revealed to correlate with charge transfers of HOMO-LUMO transitions, energy barriers of aromatic substituents rotation and the lifetime of excited states in the investigated complexes. The bathochromic shift of intensive bands in the optical spectra has been observed to occur when the functional groups are introduced into p-positions of phenyl cycles due to destabilizing HOMO levels.

Electronic Structure and Optical Properties of Boron Difluoride Dibenzoylmethane Derivatives.

Electronic structure and optical properties of boron difluoride dibenzoylmethanate BF2Dbm and its four derivatives were studied using X-ray photoelectron spectroscopy, absorption and luminescence spectroscopy, and quantum chemistry (DFT and TDDFT). In a series of the studied compounds, the relationship of molecular design and optical properties has been revealed. At the transition from BF2Dbm to BF2Dbm(OCH3)2, the HOMO-LUMO energy gap decreases, resulting in a bathochromic shift of the optical spectra.